ENST00000527168.6:n.882T>C
|
|
|
ENST00000529110.2:c.867T>C
|
ENSP00000435349.2:p.Gly289=
|
|
ENST00000529957.6:n.841T>C
|
|
|
ENST00000683366.1:c.*515T>C
|
ENSP00000507283.1:n.*515T>C
|
|
ENST00000683887.1:c.831T>C
|
ENSP00000506886.1:p.Gly277=
|
|
ENST00000684100.1:n.777T>C
|
|
|
ENST00000684126.1:n.917T>C
|
|
|
ENST00000684688.1:n.1408T>C
|
|
|
ENST00000204679.9:c.783T>C
MANE Select
|
ENSP00000204679.4:p.Gly261=
|
|
ENST00000204679.8:c.783T>C
|
ENSP00000204679.4:p.Gly261=
|
|
ENST00000527076.1:n.2006T>C
|
|
|
ENST00000527168.5:n.950T>C
|
|
|
ENST00000529957.5:n.882T>C
|
|
|
NM_032520.4:c.783T>C
|
NP_115909.1:p.Gly261=
|
|
XM_017023782.1:c.831T>C
|
XP_016879271.1:p.Gly277=
|
|
XM_017023783.1:c.423T>C
|
XP_016879272.1:p.Gly141=
|
|
NM_032520.5:c.783T>C
MANE Select
|
NP_115909.1:p.Gly261=
|
|